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1 oth a 3' --> 5' DNA helicase and a 3' --> 5' DNA exonuclease.
2 uclease 1 (hExo1), a 5'-->3' double-stranded DNA exonuclease.
3 a cyclic AMPase; and RecJ, a single-stranded DNA exonuclease.
4 chiacoli RecQ helicase family, and a 3'-->5' DNA exonuclease.
5 as previously identified as a 3'-5'-directed DNA exonuclease.
6 we show that MrfB is a Mg2+-dependent 3'-5' DNA exonuclease.
7 of proteins constitute a novel class of RNA-DNA exonucleases.
8 by RecG DNA translocase and by single-strand DNA exonucleases.
10 ted that T4 RNase H, a 5'-3' exonuclease, T4 DNA exonuclease A (DexA) and the exonuclease activity of
11 encodes 3' --> 5' DNA helicase and 3' --> 5' DNA exonuclease activities, and is implicated in the mai
18 pendent on the 5' --> 3' single-stranded (ss)DNA exonuclease activity of RecJ and the helicase activi
20 enzyme not only displays 5'-3' double strand DNA exonuclease activity, but also shows an RNase H acti
21 enzyme exhibits an aberrant double-stranded DNA exonuclease activity, intrinsically producing a 3'-t
26 unknown function), Rnh (RNase H and 5' to 3' DNA exonuclease), alpha-gt (alpha-glucosyl transferase),
29 c variants in the gene encoding the 5'-to-3' DNA exonuclease Apollo/SNM1B in 3 unrelated patients pre
31 tion study using t(14;18)-positive cell line DNA, exonuclease-based PCR detected fusion sequences at
32 changes the nature of RecBCD double-stranded DNA exonuclease by increasing the rate of digestion of t
33 Deficiency in the two major 3' single-strand DNA exonucleases, ExoI and ExoVII, stimulated hotspot mu
34 we have proposed for the other single-strand DNA exonucleases, exonuclease X may facilitate recombina
35 exhibits wild-type levels of double-stranded DNA exonuclease, helicase, and ATPase activity, its abil
36 en used to measure the degradation of DNA by DNA exonuclease I, providing data that would not be avai
40 the bacterium Escherichia coli there are 14 DNA exonucleases including exonucleases I-IX (including
42 3' repair exonuclease 1 (TREX1) is a known DNA exonuclease involved in autoimmune disorders and the
43 XO1) is a pleiotropic evolutionary conserved DNA exonuclease involved in various DNA repair pathways,
44 REX1, encoding the major mammalian 3' --> 5' DNA exonuclease, is the AGS1 gene, and AGS-causing mutat
45 9 g restriction fragments can be degraded by DNA exonucleases or ligated by T3 and T4 DNA ligases.
46 e repair exonuclease 1(TREX1), an endogenous DNA exonuclease, prevents immune activation by depleting
47 g defence in vivo, we demonstrate that viral DNA exonucleases required for phage replication trigger
50 As ExoV, it is a potent double-stranded (ds)DNA exonuclease that destroys linear DNA produced by res
51 clease VII was first identified in 1974 as a DNA exonuclease that did not require any divalent cation
52 candidate is Exo1p, a 5'-3' double stranded DNA exonuclease that has previously been implicated in D
53 The TREX1 gene encodes a highly efficient DNA exonuclease that plays an important role in maintain
55 overproduce type I IFNs owing to loss of the DNA exonuclease Trex1, inflammatory disease completely d
56 ort that p53 promotes the degradation of the DNA exonuclease TREX1, resulting in cytosolic dsDNA accu
58 on is mediated by KSHV ORF37, a homolog of a DNA exonuclease widely present in other herpesviruses bu